An Adrenalectomy Mouse Model Reflecting Clinical Features for Chronic Fatigue Syndrome

• Published in: Biomolecules (Basel, Switzerland) Switzerland), 2020-01, Vol.10 (1), p.71
• Main Authors: Lee, Jin-Seok, Jeon, Yoo-Jin, Park, Samuel-Young, Son, Chang-Gue
• Format: Article
• Language: English
• Subjects: Adrenalectomy; Adrenalectomy - methods; animal model; Animal models; Animals; Astrocytes; Brain - metabolism; Chronic fatigue syndrome; Disease Models, Animal; Drinking water; Fatigue; Fatigue Syndrome, Chronic - metabolism; Fatigue Syndrome, Chronic - physiopathology; Hippocampus - metabolism; Injection; Laboratory animals; lipopolysaccharide; Lipopolysaccharides; Lipopolysaccharides - pharmacology; Male; Medical research; Mice; Mice, Inbred ICR; Microglia; Muscle strength; Neuroendocrine system; Neurosciences; Neurosecretory Systems - metabolism; Neurosecretory Systems - physiopathology; Poly (I:C); Poly I-C - pharmacology; polyinosinic: polycytidylic acid; Prefrontal cortex; Proteins; Serotonin Plasma Membrane Transport Proteins - metabolism; Serotonin S1 receptors
• ISSN: 2218-273X; 2218-273X
• DOI: 10.3390/biom10010071

Chronic fatigue syndrome (CFS) is one of the most intractable diseases and is characterized by severe central fatigue that impairs even daily activity. To date, the pathophysiological mechanisms are uncertain and no therapies exist. Therefore, a proper animal model reflecting the clinical features of CFS is urgently required. We compared two CFS animal models most commonly used, by injection with lipopolysaccharide (LPS from O111:B4) or polyinosinic: polycytidylic acid (poly I:C), along with bilateral adrenalectomy (ADX) as another possible model. Both LPS- and poly I:C-injected mice dominantly showed depressive behaviors, while ADX led to fatigue-like performances with high pain sensitivity. In brain tissues, LPS injection notably activated microglia and the 5-hydroxytryptamine (HT) receptor in the prefrontal cortex and hippocampus. Poly I:C-injection also remarkably activated the 5-HT transporter and 5-HT receptor with a reduction in serotonin levels in the brain. ADX particularly activated astrocytes and transforming growth factor beta (TGF-β) 1 in all brain regions. Our results revealed that LPS and poly I:C animal models approximate depressive disorder more closely than CFS. We suggest that ADX is a possible method for establishing a mouse model of CFS reflecting clinical features, especially in neuroendocrine system.